Glass substrate for display cover glass and its production process

ABSTRACT

To provide a glass substrate for a display cover glass not only having excellent strength and antibacterial properties but also having a high transparency and a high visible transmittance suitable as a cover glass for a display device. A glass substrate for a display cover glass, which comprises a surface compressive stress layer and an antibacterial substance-containing layer formed on the glass substrate surface, characterized by having a ratio (T 1 /T 2 ) of the transmittance T 1  at a wavelength of 428 nm to the transmittance T 2  at a wavelength of 650 nm of the glass substrate of at least 0.95, and a transmittance at a wavelength of 428 nm of at least 86% when the thickness of the glass substrate is from 0.1 to 3.0 mm.

TECHNICAL FIELD

The present invention relates to a glass substrate useful for a coverglass of display devices, typically display devices having inputfunctions, such as cell-phones, personal digital assistant (PDAs) andtouch panels, and its production process.

BACKGROUND ART

In recent years, a cover glass (protective glass) has been frequentlyused to protect a display and to improve its appearance, on displaydevices having input functions such as mobile devices such ascell-phones and PDAs and touch panels.

Such a glass substrate for a display cover glass is required to be thinand to have high strength, and a glass substrate having increasedstrength by a chemical tempering method is commonly used.

Further, for such mobile devices and display devices with touch panels,hygiene management has been required.

To ticket vending machines at stations and ATMs used in the generalpublic, and display devices with touch panels such as devices used inmedical care facilities, due to their usage environment, variousbacteria are very likely to be attached. Further, mobile devices alsohave the similar problem, since they are very frequently used althoughthe users are limited.

Accordingly, for such devices and apparatus, it has been desired toimpart antibacterial properties particularly to a glass substrate for adisplay cover glass which people very frequently touch.

In regard to this, glass excellent in antibacterial properties and alsoexcellent in the strength is disclosed in JP-A-11-228186 (PatentDocument 1). This document discloses that antibacterial properties andhigh strength (bending strength) can be imparted to glass by treatingglass containing sodium with a molten salt of silver nitrate andpotassium nitrate to replace sodium ions contained in glass with both ofpotassium ions and silver ions. Further, to provide glass also excellentin the transparency, it is considered preferable that the proportion(weight ratio) of a compound capable of donating M⁺ which replacessodium ions of glass, to an antibacterial substance, is within aspecific range.

PRIOR ART DOCUMENT Patent Document

Patent Document 1: JP-A-11-228186

DISCLOSURE OF INVENTION Technical Problem

However, the present inventors have prepared the soda-lime glass A asdisclosed in Patent Document 1 and prepared the glass in Example withgood transparency to confirm the transparency, whereupon it was found tohave a low transmittance in the visible region and be insufficient as aglass substrate for a display cover glass. The reason is considered thatsilver ions are diffused quickly as compared with potassium ions, andwhen treatment is conducted to obtain a desired strength, silver ionswill excessively be diffused in glass, and the diffused silver ions areformed into a colloid, whereby glass is colored and has absorptivity toa specific wavelength in the visible region.

Under these circumstances, it is an object of the present invention toprovide a glass substrate for a display cover glass not only having ahigh strength and excellent antibacterial properties but also having ahigh transparency and a high visible transmittance suitable as a coverglass for display devices, and its production process.

Solution to Problem

The present inventors have focused attention on that formation of silverin a silver ion diffusion layer which imparts antibacterial propertiesto glass, into a colloid, inhibits the transparency of glass, and theyhave found that a strength, antibacterial properties and a transparencysuitable as a glass substrate for a display cover glass can be obtainedby controlling the transmittance in the vicinity of 428 nm which is theabsorption wavelength of silver colloid to be within a specific range.

That is, the glass substrate for a display cover glass of the presentinvention comprises a surface compressive stress layer and anantibacterial substance-containing layer on the glass substrate surface,and is characterized by having a ratio (T1/T2) of the transmittance T1at a wavelength of 428 nm to the transmittance T2 at a wavelength of 650nm of the glass substrate of at least 0.95, and a transmittance at awavelength of 428 nm of at least 86% when the thickness of the glasssubstrate is from 0.1 to 3.0 mm.

Further, the glass substrate for a display cover glass of the presentinvention is characterized in that the glass substrate has a glasscomposition comprising, as represented by mol % as calculated as oxides,from 55 to 80% of SiO₂, from 0.1 to 15% of Al₂O₃, from 0 to 15% of B₂O₃,from 0 to 10% of ZnO, from 0.1 to 15% of Na₂O, from 0 to 10% of K₂O, andfrom 0 to 16% of MgO+CaO.

Further, the glass substrate for a display cover glass of the presentinvention is characterized in that the surface compressive stress layeron the glass substrate surface is formed by chemical tempering, and thesurface compressive stress layer has a depth of at least 3 μm and asurface compressive stress of a least 250 MPa.

Further, the glass substrate for a display cover glass of the presentinvention is characterized in that the antibacterialsubstance-containing layer is a silver ion diffusion layer having silverions diffused in the glass substrate surface.

Further, the glass substrate for a display cover glass of the presentinvention is characterized in that the silver ion diffusion layer has asilver amount of from 0.2 to 100 μg/cm² at a depth of 40 μm from theglass substrate surface.

Further, the glass substrate for a display cover glass of the presentinvention is characterized in that the glass substrate is plate-formedby a float process.

Further, the glass substrate for a display cover glass of the presentinvention is characterized in that it is used for a cover glass of atouch panel display.

Further, the present invention provides a display device, which uses theabove glass substrate for a display cover glass as a front glass of adisplay.

The process for producing a glass substrate for a display cover glass ofthe present invention comprises a step of chemically tempering a glasssubstrate in a molten salt containing at least KNO₃, a step of cleaningthe chemically tempered glass substrate, a step of forming a silver filmon the surface of the cleaned glass substrate, a step of subjecting theglass substrate having the silver film formed thereon to heat treatmentto diffuse silver ions from the glass substrate surface to the inside,and a step of washing and removing silver remaining on the surface, notdiffused in the inside of the glass substrate in the above step ofdiffusing silver ions.

Further, the process for producing a glass substrate for a display coverglass of the present invention comprises a step of plate-forming a glasssubstrate, a step of chemically tempering the plate-formed glasssubstrate in a molten salt containing at least KNO₃, a step of cleaningthe chemically tempered glass substrate, a step of forming a silver filmon the surface of the cleaned glass substrate, a step of subjecting theglass substrate having the silver film formed thereon to heat treatmentto diffuse silver ions from the glass substrate surface to the inside,and a step of washing and removing silver remaining on the surface, notdiffused in the inside of the glass substrate in the above step ofdiffusing silver ions.

Further, the process is characterized in that the step of plate-forminga glass substrate is carried out by a float process.

Further, the process is characterized in that the step of diffusingsilver ions involves a step of subjecting the glass substrate having thesilver film formed thereon to heat treatment at from 300 to 475° C.

Advantageous Effects of Invention

According to the present invention, a glass substrate for a displaycover glass not only having a high strength and excellent antibacterialproperties, but also having a high transparency and a high visibletransmittance by suppressing coloring of glass due to silver colloid,can be obtained.

DESCRIPTION OF EMBODIMENTS

The glass substrate for a display cover glass of the present inventioncomprises a surface compressive stress layer on the substrate surface.By having the surface compressive stress layer on the glass substratesurface, the strength of the glass substrate can dramatically beimproved.

As a method to form a compressive stress layer on the glass substratesurface, an air quenching tempering method (physical tempering method)wherein the surface of a glass substrate heated to near the softeningpoint is quenched by air cooling or the like and a chemical temperingmethod wherein alkali metal ion having a small ion radius (typically Liions or Na ions) on the surface of a glass substrate are exchanged withalkali metal ions having a larger ion radius (typically K ions) by ionexchange at a temperature of at most the glass transition point, may beapplied.

Particularly in a case of forming a surface compressive stress layer ona thin glass substrate, if the air quenching tempering method isapplied, the temperature difference between the surface and the insidetends not to arise, and it is thereby difficult to form a surfacecompressive stress layer, and desired strength can hardly be obtained.Therefore, it is preferred to form a surface compressive stress layer bythe chemical tempering method.

The thickness of the glass substrate for a display cover glass of thepresent invention is typically preferably from 0.2 to 3.0 mm when weightsaving is particularly required, for example, in the case of being usedfor mobile devices. If it is less than 0.2 mm, even though the chemicaltempering is carried out, the desired strength may not be obtained fromthe viewpoint of the strength for practical use. If it exceeds 3.0 mm,such is unfavorable in view of the weight saving. It is more preferablyfrom 0.5 to 1.5 mm.

When weight saving is not particularly required, for example, in thecase of being used for fixed devices without being carried, it ispossible to apply the present invention even when the thickness of theglass substrate exceeds 3.0 mm for example. It is possible to apply thephysical tempering when the thickness of the glass substrate exceeds 3.0mm, however, the surface compressive stress imparted by the physicaltempering is commonly at a level of from 100 to 150 MPa, and accordinglywhen a further higher surface compressive stress is required, a glasssubstrate having a higher strength can be obtained by forming a surfacecompressive stress layer by the chemical tempering.

The surface compressive stress layer of the glass substrate for adisplay cover glass of the present invention preferably has a depth ofat least 3 μm. If the depth is less than 3 μm, the strength isinsufficient as a glass substrate for a display cover glass, and thescratch resistance (likelihood of indentations when injured) of theglass substrate surface tends to be deteriorated. The depth of thesurface compressive stress layer is preferably from 5 μm to 100 μm, morepreferably from 7 to 80 μm.

The surface compressive stress of the glass substrate for a displaycover glass of the present invention is preferably from 250 to 1,050MPa. If the surface compressive stress is less than 250 MPa, thestrength is insufficient as a glass substrate for a display cover glass,and the scratch resistance of the glass substrate surface tends to bedeteriorated. Further, if it exceeds 1,050 MPa, the internal tensilestress tends to be large, and when cracks progress into the inside ofthe glass substrate e.g. by an impact, explosive destruction may occur,such being unfavorable in view of the safety. The surface compressivestress is preferably from 300 to 800 MPa, more preferably from 350 to750 MPa.

The glass substrate for a display cover glass of the present inventioncomprises an antibacterial substance-containing layer on the substratesurface. By having the antibacterial substance-containing layer on theglass substrate surface, antibacterial functions can be imparted to theglass substrate.

The antibacterial substance-containing layer formed on the glasssubstrate surface is roughly classified into a layer containing silveritself and a silver ion diffusion layer. As a method of forming thelayer containing silver itself, a method of mixing silver with glassmaterials, followed by melt forming, and a method of forming a coatinglayer containing silver on the glass substrate surface, have been known.On the other hand, as a method of forming the silver ion diffusionlayer, a method of coating the glass substrate surface with a liquidcontaining silver, followed by heat treatment to form the silver iondiffusion layer over from the glass substrate surface to the inside ofthe substrate, has been known. By the method of forming the silver iondiffusion layer, as compared with the method of forming the layercontaining silver itself, the antibacterial properties will not beeliminated in a short time e.g. by abrasions, and the quality of theglass substrate surface will not remarkably be changed. Accordingly, toimpart antibacterial functions to the glass substrate for a displaycover glass of the present invention, it is preferred to employ themethod of forming the silver ion diffusion layer. Further, in the methodof forming the silver ion diffusion layer, as a method of forming silveron the glass substrate surface, in addition to the above method ofcoating the glass substrate surface with a liquid containing silver, amethod of spray pyrolysis of a liquid containing a silver salt or amethod by vacuum sputtering may, for example, be mentioned.

Further, as the antibacterial substance-containing layer, a layer of anatural antibacterial agent represented by Japanese horseradish, a metalantibacterial agent represented by copper or zinc, an oxideantibacterial agent represented by titanium oxide, other than silver,may be formed by a known method.

The silver ion diffusion layer which is the antibacterialsubstance-containing layer of the glass substrate for a display coverglass of the present invention preferably has a silver amount of from0.2 to 100 μg/cm² at a depth of 40 μm from the glass substrate surface.If the silver amount of the glass substrate is less than 0.2 μg/cm², nosufficient antibacterial effects will be obtained. Further, if itexceeds 100 μg/cm², the silver amount diffused in the silver iondiffusion layer tends to be too large, whereby glass may be colored dueto silver colloid. The silver amount is preferably from 0.4 to 80μg/cm², more preferably from 0.6 to 60 μg/cm², particularly preferablyfrom 0.8 to 20 μm/cm², and most preferably from 1.0 to 15 μg/cm².

The present inventors have confirmed the relation between the silveramount of the glass substrate and the antibacterial effect by thefollowing method. Further, plate-form borosilicate glass (PYREX(registered trademark)) was prepared, and antibacterialactivity-imparted glass substrates having silver amounts of 0.2, 0.4 and0.6 μg/cm², respectively, at a depth of 40 μm from the glass substratesurface, were prepared. With respect to these glass substrates, inaccordance with JIS Z2801 (test for antibacterial activity), the numberof bacteria (Escherichia coli. Staphylococcus aureus) in glass samples24 hours later under the conditions specified, was confirmed. Thesterilization ratio was calculated by comparison with a non-treated filmtreated under the same conditions. As a result, with respect to theglass substrate with a silver amount of 0.2 μg/cm², 90% or more bacteriawere killed, and with respect to the glass substrates with silveramounts of 0.4 and 0.6 μg/cm², 99% or more bacteria were killed.Therefore, the present inventors have considered that when the silveramount is at least 0.2 μg/cm² at a depth of 40 μm from the glasssubstrate surface, the glass substrate has an antibacterial effect.

At a portion where two layers of the surface compressive stress layerand the antibacterial substance-containing layer are formed, regardlessof the order of formation, the two layers are blended together in manycases at least on the outermost surface of the glass substrate, but theymay be laminated in two layers in order of the formation.

Not only the glass substrate surface has both of the surface compressivestress layer and the antibacterial substance-containing layer, but alsoone part of the glass substrate surface comprises the surfacecompressive stress layer and the other part comprises the antibacterialsubstance-containing layer. Further, one part of the glass substratesurface comprises both of the surface compressive stress layer and theantibacterial substance-containing layer, and the other part compriseseither one of the surface compressive stress layer and the antibacterialsubstance-containing layer. Further, on the glass substrate surface,there may be a portion where neither of the surface compressive stresslayer nor the antibacterial substance-containing layer is formed.

The glass substrate for a display cover glass of the present inventionhas a ratio (transmittance ratio (T1/T2)) of the transmittance T1 at awavelength of 428 nm to the transmittance T2 at a wavelength of 650 nmof the glass substrate of at least 0.95, and has a transmittance of atleast 86% at wavelength of 428 nm when the thickness of the glasssubstrate is from 0.1 to 3.0 mm.

The reason why a wavelength of 428 nm is employed is that coloring ofglass by silver colloid can directly be evaluated since the absorptionwavelength when glass is colored by silver colloid reaches the localmaximum in the vicinity of this wavelength. Further, the reason why awavelength of 650 nm is employed is that if glass is colored by silvercolloid, the transmittance is influenced not only in the waveband in thevicinity of 428 nm but also in a range of about 100 nm around thiswavelength, and accordingly the wavelength of 650 nm is selected as itis the wavelength in the visible region which is not influenced by theabove. Further, the ratio (T1/T2) of the transmittance T1 at awavelength of 428 nm to the transmittance T2 at a wavelength of 650 nmof the glass substrate is at least 0.95, and the transmittance at awavelength of 428 nm is at least 86% when the thickness of the glasssubstrate is from 0.1 to 3.0 mm, and by having such transmittancecharacteristics, a glass substrate free from coloring by silver colloidand having a high transparency and a high visible transmittance suitableas a glass substrate for a display cover glass can be obtained.

If the transmittance at a wavelength of 428 nm is less than 86% when thethickness of the glass substrate is from 0.1 to 3.0 mm, or if the ratio(T1/T2) of the transmittance T1 at a wavelength of 428 nm to thetransmittance T1 at a wavelength of 650 nm of the glass substrate isless than 0.95, the transparency and the visible transmittance will below to such an extent that coloring of glass due to silver colloid isvisually recognized, and if such a glass substrate is used for displaydevices, the visibility of the display screen will be lowered, suchbeing unfavorable.

The glass substrate for a display cover glass of the present inventioncan be obtained by subjecting a plate-formed glass substrate to thechemical tempering treatment and the antibacterial treatment.

As a method of plate-forming the glass substrate, a float process, adown draw process, a press method or the like may be employed, andparticularly when a large quantity of glass is to be plate-formed at alow cost, the float process is preferably employed.

In a case where the glass-substrate plate-formed by the float process isused without polishing, it is preferred to provide the antibacterialsubstance-containing layer on the surface opposite to the surface(hereinafter referred to as the tin-side surface) which was in contactwith molten tin in the float process. This is because as on the glasssubstrate surface on the side of the tin-side surface, a tin componentis diffused in glass, and if the silver ion diffusion layer is formed onthis surface, silver in the silver ion diffusion layer is reduced by thetin component and is formed into a colloid, thereby colors glass.

However, in a case where it is necessary to form an electrode on theglass substrate surface, if an electrode is formed on the tin-sidesurface, a problem may arise such that glass is colored by the reactionof electrode material components and the tin component in the glasssubstrate. Accordingly, the surface compressive stress layer and theantibacterial substance-containing layer are provided on the tin-sidesurface. On that occasion, in order to suppress formation of silver inthe silver ion diffusion layer on the tin-side surface into a colloid,in the antibacterial treatment, it is preferred to carry out the heattreatment at a temperature of at most 425° C. Further, in a case offorming an electrode on the glass substrate surface using e.g. a silverpaste containing silver particles and low melting point glass as themain components, a firing step at a temperature higher than 425° C. isnecessary, and in such a case, formation of a silver colloid can beavoided by forming the antibacterial substance-containing layer afterformation of the electrode.

Now, the composition of the glass substrate of the present inventionwill be described with reference to contents as represented by mol %unless otherwise specified.

SiO₂ is an essential component to constitute a glass matrix. If itscontent is less than 55%, stability of glass deteriorates, or weatherresistance deteriorates. It is preferably at least 60%. Further, if itexceeds 80%, the viscosity of glass will increase, and a meltingproperty will remarkably be lowered. It is preferably at most 75%,typically at most 73%.

Al₂O₃ is an essential component to improve a rate of ion exchange. Ifits content is less than 0.1%, the rate of ion exchange tends to be low.It is preferably at least 1%, typically at least 1.5%. If the Al₂O₃content exceeds 15%, the viscosity of glass tends to be high, and ittends to be difficult to melt glass homogeneously. It is preferably atmost 11%, more preferably at most 8%.

B₂O₃ may be contained up to 15% for example, to improve the meltingproperty at high temperature or to improve the glass strength. If itscontent exceeds 15%, glass tends to be unstable. It is preferably atmost 10%, more preferably at most 8%. Further, in order to increase thesilver amount of the glass substrate surface by the antibacterialtreatment, it is preferably at most 5%, and it is more preferred that noB₂O₃ is contained.

ZnO may be contained up to 10% for example, to improve the meltingproperty of glass at high temperature. If its content exceeds 10%, glasstends to be unstable. It is preferably at most 8%, more preferably atmost 6%. Further, in order to increase the silver amount of the glasssubstrate surface by the antibacterial treatment, it is preferably atmost 3%, and it is more preferred that no ZnO is contained.

Na₂O is an essential component to form the surface compressive stresslayer by ion exchange and to improve the melting property of the glass.If its content is less than 0.1%, it tends to be difficult to form adesired surface compressive layer by ion exchange. It is preferably atleast 3%, typically at least 6%. If the Na₂O content exceeds 15%, Tgi.e. the strain point tends to be low, or the weather resistance tendsto be low. If Tg is low, the stress tends to be relaxed at the time ofthe chemical tempering, whereby it tends to be difficult to obtaindesired chemical tempering properties. The content is preferably at most14%, typically at most 13%.

K₂O is a component to improve the melting property and to increase therate of ion exchange by the chemical tempering thereby to obtain desiredsurface compressive stress and surface compressive stress layer, and ispreferably contained in an amount of at most 10%. Its content ispreferably at least 0.1%, more preferably at least 2%, typically atleast 3%. If the K₂O content exceeds 10%, the weather resistance tendsto be low. It is preferably at most 8%, typically at most 6%.

The alkaline earth metal oxide is a component to improve the meltingproperty and is a component effective to control Tg i.e. the strainpoint as well.

Each of MgO and CaO has a relatively small effect to lower the rate ofion exchange, and they may be contained in a content of MgO+CaO of atmost 16%. If the content of MgO+CaO exceeds 16%, the rate of ionexchange tends to be low, glass tends to be devitrified, or the strainpoint tends to be too low. It is preferably at most 15%, more preferablyat most 13%.

The glass substrate of the present invention typically has a glasscomposition comprising, as represented by mol % as calculated as oxides,from 55 to 80% of SiO₂, from 0.1 to 15% of Al₂O₃, from 0 to 15% of B₂O₃,from 0 to 10% of ZnO, from 0.1 to 15% of Na₂O, from 0 to 10% of K₂O andfrom 0 to 16% of MgO+CaO.

The glass substrate of the present invention essentially comprises theabove components but may contain other components within a range not toimpair the object of the present invention. When such components arecontained, the total content of these components is preferably at most10%, typically at most 5%. Such other components will be describedbelow.

BaO and SrO have the highest effect to lower the rate of ion exchangeamong alkaline earth metal oxides, and accordingly when they arecontained, their content is preferably less than 1%.

ZrO₂ is not essential but may be contained up to 5% so as to increasethe rate of ion exchange. If its content exceeds 5%, the effect ofincreasing the rate of ion exchange will no longer increase, and themelting property tends to be deteriorated, whereby stones may remain inglass in some cases. When ZrO₂ is contained, its content is preferablyat least 0.5%, typically at least 1%.

As a refining agent at the time of melting glass, SO₃, chlorides,fluorides, Sb₂O₃, As₂O₃ and the like may appropriately be contained.

Further, it is preferred to reduce contamination of impurities inmaterials, such as Fe₂O₃, NiO and Cr₂O₃ having absorption in the visibleregion, as far as possible, and each content is preferably at most0.15%, more preferably at most 0.05% as represented by mass %.

The glass substrate for a display cover glass of the present inventionis suitably used as a display front glass of display devices havinginput functions such as touch panel displays. The glass substrate for acover glass of touch panel displays is required to have high visibilityas a display device, a high strength capable of enduring the load whenoperated by touching, and antibacterial properties to maintain hygieneeven though the general public use, and the glass substrate for adisplay cover glass of the present invention sufficiently has theseproperties.

Further, by using the glass substrate for a display cover glass as thefront glass of displays, a display device having a high visibility as adisplay device, a high strength capable of enduring the load whenoperated or carried, and antibacterial properties to maintain hygiene,can be obtained.

Now, the process for producing the glass substrate for a display coverglass of the present invention will be described.

The process for producing a glass substrate for a display cover glass ofthe present invention comprises a step of chemically tempering a glasssubstrate in a molten salt containing at least KNO₃, a step of cleaningthe chemically tempered glass substrate, a step of forming a silver filmon the surface of the cleaned glass substrate, a step of subjecting theglass substrate having the silver film formed thereon to heat treatmentto diffuse silver ions from the glass substrate surface to the inside,and a step of washing and removing silver remaining on the surface, notdiffused in the inside of the glass substrate in the above step ofdiffusing silver ions.

Further, the process for producing a glass substrate for a display coverglass of the present invention comprises a step of plate-forming a glasssubstrate, a step of chemically tempering the plate-formed glasssubstrate in a molten salt containing at least KNO₃, a step of cleaningthe chemically tempered glass substrate, a step of forming a silver filmon the surface of the cleaned glass substrate, a step of subjecting theglass substrate having the silver film formed thereon to heat treatmentto diffuse silver ions from the glass substrate surface to the inside,and a step of washing and removing silver remaining on the surface, notdiffused into the inside of the glass substrate in the above step ofdiffusing silver ions.

The step of plate-forming a glass substrate is not particularly limitedin detail, however, for example, the plate-formed glass substrate isproduced in such a manner that various materials are properly blended,heated at about 1,400 to 1,600° C. and melted, homogenized by deforming,stirring or the like, and formed into a plate by a known float process,down draw process or press method, annealed and then cut into a desiredsize, followed by polishing.

The chemical tempering step is not particularly limited so long as Na₂Oon the glass substrate surface can be ion-exchanged with K₂O in themolten salt, and for example, a method of dipping the glass substrate ina heated molten salt containing potassium nitrate (KNO₃) may bementioned.

The conditions to form the chemically tempered layer (surfacecompressive stress layer) having a desired surface compressive stress onthe glass substrate vary depending upon the thickness of the glasssubstrate, however, it is typical that the glass substrate is dipped ina molten salt containing KNO₃ at from 400 to 550° C. for from 2 to 20hours. From the economical viewpoint, it is preferred to dip the glasssubstrate in the molten salt at from 400 to 500° C. for from 2 to 16hours, more preferably at 400 to 500° C. for from 2 to 10 hours.

In the cleaning step, the molten salt containing potassium nitrate(KNO₃) used in the chemical tempering step and stains are removed fromthe glass substrate surface. This is because if the glass substratesurface is stained, in the step of forming a silver film as thefollowing step, unevenness or missing may occur on the silver film. Thecleaning method is not particularly limited and may, for example, be amethod of spraying the glass substrate with distilled water or the like,a method of dipping the glass substrate in a water bath and applyingultrasonic vibration, or a method of scrubbing the glass substrate witha polishing agent.

The step of forming a silver film on the surface of the glass substrateand the step of diffusing silver ions are steps to form theantibacterial substance-containing layer on the glass substrate surface.

The step of forming a silver film may be a method of mixing silver withglass materials, followed by melt forming, a method of forming a coatinglayer containing silver on the glass substrate surface, or a method ofcoating the glass substrate surface with a liquid containing silver,followed by heat treatment to form a silver ion diffusion layer overfrom the glass substrate surface to the inside of the substrate, and inview of the productivity and the equipment cost, it is preferred toemploy the method of forming a silver ion diffusion layer.

The heat temperature conditions in the step of diffusing silver ionsvary depending on the composition of the glass substrate, the silveramount applied, and heating conditions for heat diffusion, and preferredis treatment at from 250 to 500° C. If the heating temperature is lessthan 250° C., the diffusion rate tends to be low, and it will take longto diffuse silver to develop the antibacterial effect, such beinguneconomical. If it exceeds 500° C., a large amount of silver will bediffused even in short time and is formed into silver colloid, wherebyglass is colored and absorbs the wavelength in the vicinity of 428 nm,such being unfavorable. The more preferred heating temperature is from300 to 475° C. If it is at least 300° C., silver to develop theantibacterial effect can be diffused in a short time, and if it is atmost 475° C., a larger amount of silver can be diffused withoutcoloring.

The step of washing and removing silver remaining on the surface iscarried out to remove the silver residue not diffused in the glassinside, formed after heat diffusion of silver. The washing method is notparticularly limited, and for example, it is preferred to wash the glasssubstrate with a solution containing any of HNO₃, FeCl₃, Fe(NO₃)₃, HCl,H₂SO₄ and H₂O₂.

To obtain a glass substrate for a display cover glass of the presentinvention, which comprises a surface compressive stress layer and anantibacterial substance-containing layer on the glass substrate surface,and which has predetermined transmittance characteristics, theproduction process is not limited to the above-described productionprocess, and it is also possible to conduct chemical tempering treatmentafter the glass substrate is subjected to the antibacterial treatment.

However, it is not preferred to conduct the chemical tempering treatmentand the antibacterial treatment simultaneously on the glass substrate.If these treatments are conducted simultaneously, the treatment step andthe cleaning step can be reduced, such being advantageous in that theglass substrate can be produced at a low cost. However, when thediffusion rates of silver ions and potassium ions into the glasssubstrate surface are compared, the diffusion rate of silver ions ishigher than that of potassium ions. Accordingly, if the chemicaltempering treatment is conducted for a time required to form the surfacecompressive stress layer to obtain the desired strength, silver ionswill excessively be diffused in the glass substrate surface, wherebycoloring due to silver colloid will occur, and optical propertiesrequired for a glass substrate for a display cover glass, that is, theabove-described transmittance characteristics will not be obtained.

From the above reason, to obtain the glass substrate for a display coverglass of the present invention, the chemical tempering treatment and theantibacterial treatment should be conducted separately.

EXAMPLES

Now, the present invention will be described in further detail withreference to Examples of the present invention and Comparative Examples.However, it should be understood that the present invention is by nomeans restricted to the following Examples.

In the following Examples and Comparative Examples, glasses A, B, C andD having the glass compositions as identified in Table 1 were used. InTable 1, the blanks in the respective components mean a content of 0 mol%.

With respect to each glass, usually used glass materials such as oxides,hydroxides, carbonates and nitrates were appropriately selected so as tobe compositions as represented by mol % shown in columns of therespective components in Table 1, such materials were weighed so as tobe 800 g of glass and mixed. Then, the mixture was put in a platinumcrucible, the platinum crucible was put in a resistant heat typeelectric furnace at 1,600° C., and the mixture was melted for threehours, refined and homogenized, and cast in a mold and annealed at apredetermined temperature to obtain a glass block. The glass block wascut into a size of 40 mm×40 mm×about 0.3 to 1.0 mm in thickness andpolished, and finally both surfaces were mirror polished to obtain aplate-form glass. With respect to glass A, the plate forming wasconducted by the float process, and the plate was cut into a size of 40mm×40 mm and polished, and finally both surfaces were mirror polished toobtain a plate-form glass substrate.

TABLE 1 Mol % Glass A Glass B Glass C Glass D SiO₂ 72 64.5 71.3 70.6Al₂O₃ 1.1 6 2 2.6 B₂O₃ 7.7 ZnO 4.4 Na₂O 12.6 12 10.8 6.7 K₂O 0.2 4 4.64.7 MgO 5.5 11 10.4 CaO 8.6 0.11 0.3 SrO 0.06 0.03 BaO 0.04 0.02 TiO₂3.2 ZrO₂ 2.5 0.5 Sb₂O₃ 0.1 Fe₂O₃ 0.005 Na₂SO₄ 0.09

Then, each of the obtained glass substrates was dipped in a molten saltcontaining KNO₃ for a predetermined time to obtain a glass substratehaving a surface compressive stress layer on its surface. Variousconditions (molten salt concentration, time and temperature) for thechemical tempering treatment in Examples and Comparative Examples are asshown in Tables 2 to 5. The surface compressive stress of the glasssubstrate and the depth of the surface compressive stress layer weremeasured by a surface stress meter (manufactured by Orihara SeisakushoCorporation, FSM-6000). Further, the transmittance and the transmittanceratio (T1/T2) were calculated from the spectral transmittance obtainedby using an ultraviolet near-infrared spectrophotometer (manufactured byJASCO Corporation, V570).

Then, antibacterial treatment was conducted on each glass substratesubjected to the chemical tempering treatment. The specific treatmentmethod is as follows. On the chemically tempered surface of the glasssubstrate, a sponge was impregnated with a solution (cerium oxideconcentration: 1 mass %) having cerium oxide (grain size #5000 by JISR6001) dispersed in pure water, and the silver film-formed surface wasevenly rubbed and cleaned using the sponge (from about 10 to about 30seconds to the substrate of 40 mm×40 mm). On that occasion, it was notnecessary to apply a strong force, and the glass surface could be madeto be a clean surface without stains by a force at the same level asusual cleaning or lighter. After cleaning, the glass substrate wasrinsed with water so that the polishing agent would not remain. Then, astannous chloride aqueous solution (one having 1 g of stannous chlorideput and dissolved in 1,000 ml of distilled water) as an activating agentwas sprayed or run on and was brought into contact with the glasssubstrate, and then immediately discharged, and the glass substrate wascleaned with pure water.

Then, an aqueous ammonia solution and potassium hydroxide were added toa solution having silver nitrate dissolved in pure water to prepare asilver preparation. The silver concentration in the silver preparationwas 0.67 g as calculated as the mass of AgNO₃ contained in 100 ml of thesilver preparation. Glucose as a reducing agent was added to the silverpreparation to prepare a solution, which was poured into a pallet inwhich the glass substrate was placed, and the glass substrate was leftto stand for from 30 seconds to 120 seconds in a state where it wasimmersed in the solution, whereby a silver mirror surface was formed onthe glass substrate. Here, the reason why potassium hydroxide was addedis to adjust the acidic silver nitrate solution to be alkaline therebyto accelerate oxidation of the reducing liquid. The alkaline solution isnot limited to potassium hydroxide so long as it can adjust the silvernitrate solution to be alkaline. Although addition of the aqueousammonia solution alone has the same effect, potassium hydroxide was usedin combination to reduce the ammonia odor in the process.

Then, the silver mirror surface was rinsed with pure water and dried,and then the glass substrate was heated from room temperature to thepredetermined firing temperature (250 to 500° C.) in an electric furnaceat a rate of 200° C./h to carry out heat treatment for a predeterminedtime. After the heat treatment, the silver residue attached to glass wascompletely removed by using a small amount of nitric acid (for example,2 mol/L), and then the glass substrate was washed with pure water anddried to obtain a glass substrate subjected to chemical temperingtreatment and antibacterial treatment. Of the obtained glass substratesubjected to chemical tempering treatment and antibacterial treatment,chemical tempering properties (the depth of the surface compressivestress layer and the surface compressive stress), the transmittance at awavelength of 428 nm, the transmittance ratio (T1/T2) and the silveramount (fluorescent X-ray Ag intensity) diffused in the glass substratesurface were measured.

The silver amount diffused in the glass substrate surface was measuredby a fluorescent X-ray measuring apparatus (manufactured by RigakuCorporation, ZSX Primus 2). First, the Ag-Lα intensity of asilver-plated mirror with a known silver amount was measured by usingthe fluorescent X-ray measuring apparatus to prepare a calibration curveof the silver amount and the Ag-Lα intensity. Further, the Ag-Lαintensity of each of the glass substrates in Examples and ComparativeExamples was measured, and the silver amount was determined bycalculation from the measured relative intensity. With respect to theAg-Lα intensity, analysis at a depth of about 40 μm in glass ispossible, and this measured relative value was regarded as the measuredvalue of the silver amount diffused from the glass substrate surface tothe depth of 40 μm.

The above obtained chemical tempering conditions, antibacterialtreatment conditions and glass substrate properties in Examples andComparative Examples are shown in Tables 2 to 5. In Tables, Examples 1to 5 and 8 to 18 are Examples of the present invention, and Examples 6,7 and 19 to 21 are Comparative Examples. Further, in Examples 19 to 21which are Comparative Examples, the chemical tempering treatment and theantibacterial treatment were conducted simultaneously under thetreatment conditions as described in Examples 4, 5 and 7 inJP-A-11-228186, respectively. That is, as the method of the chemicaltempering treatment and the antibacterial treatment, the glass substratewas dipped in a molten salt containing KNO₃ and AgNO₃ for apredetermined time, washed with pure water and then dried to obtain aglass substrate comprising a surface compressive stress layer and anantibacterial substance-containing layer on its surface.

TABLE 2 Ex. 1 Ex. 2 Ex. 3 Ex. 4 Ex. 5 Ex. 6 Ex. 7 Glass Type of glassGlass A Glass A Glass A Glass A Glass A Glass A Glass A substrateThickness (mm) 0.32 0.32 0.32 0.32 0.32 0.32 0.32 Chemical KNO₃ (mass %)85 90 94 99 96 — 70 tempering NaNO₃ (mass %) 15 10 6 1 4 — 30 conditionsTemperature (° C.) 420 420 420 420 420 — 420 Time (h) 5.8 23.1 5.8 194.7 — 27.2 Substrate Surface compressive 325 403 457 601 559 0 241properties stress (MPa) after chemical Depth of surface 9 16 9 17 8 0 15tempering compressive stress layer (μm) Transmittance: 91 91 91 91 91 9191 428 nm (%) Transmittance ratio: 0.996 0.996 0.996 0.996 0.996 0.9960.996 428 nm/650 nm Fluorescent X-ray 0 0 0 0 0 0 0 Ag intensity(μm/cm²) Antibacterial Antibacterial Polished Polished Polished PolishedPolished Polished Polished treatment surface surface surface surfacesurface surface surface surface conditions Firing 350 350 350 350 350350 350 temperature (° C.) Firing time (h) 15 15 15 15 15 15 15 GlassSurface compressive 326 360 433 512 515 0 220 substrate stress (MPa)properties Depth of surface 8 17 8 17 8 0 17 (after chemical compressivetempering and stress layer (μm) antibacterial Transmittance: 89.0 88.790.6 90.1 90.2 90.7 84.3 treatment) 428 nm (%) Transmittance ratio:0.983 0.980 0.998 0.995 0.996 0.994 0.933 428 nm/650 nm FluorescentX-ray 4.2 5.5 4.2 2.4 1.9 4.3 8.2 Ag intensity (μg/cm²)

TABLE 3 Ex. 8 Ex. 9 Ex. 10 Ex. 11 Ex. 12 Glass Type of glass Glass BGlass B Glass B Glass B Glass B substrate Thickness (mm) 0.97 0.97 0.970.97 0.97 Chemical KNO₃ (mass %) 95 95 98 100 100 tempering NaNO₃ (mass%) 5 5 2 0 0 conditions Temperature (° C.) 400 450 425 400 450 Time (h)6 10 6 6 6 Substrate Surface compressive 544 513 673 906 808 propertiesstress (MPa) after chemical Depth of surface 31 69 42 31 54 temperingcompressive stress layer (μm) Transmittance: 90.6 90.6 90.6 90.6 90.6428 nm (%) Transmittance ratio: 0.993 0.993 0.993 0.993 0.993 428 nm/650nm Fluorescent X-ray 0 0 0 0 0 Ag intensity (μm/cm²) AntibacterialAntibacterial Polished Polished Polished Polished Polished treatmentsurface surface surface surface surface surface conditions Firing 350350 350 350 350 temperature (° C.) Firing time (h) 15 15 15 15 15 GlassSurface compressive 508 508 655 857 790 substrate stress (MPa)properties Depth of surface 31 68 42 30 54 (after chemical compressivetempering and stress layer (μm) antibacterial Transmittance: 91.1 91.091.1 91.3 88.4 treatment) 428 nm (%) Transmittance ratio: 0.993 0.9940.993 0.991 0.987 428 nm/650 nm Fluorescent X-ray 1.1 1.1 1.0 1.1 1.3 Agintensity (μg/cm²)

TABLE 4 Ex. 13 Ex. 14 Ex. 15 Ex. 16 Ex. 17 Ex. 18 Glass Type of glassGlass C Glass C Glass C Glass D Glass D Glass D substrate Thickness (mm)0.98 0.98 0.98 0.89 0.89 0.89 Chemical KNO₃ (mass %) 100 98 100 100 98100 tempering NaNO₃ (mass %) 0 2 0 0 2 0 conditions Temperature (° C.)450 400 375 450 400 375 Time (h) 10 10 10 10 10 10 Substrate Surfacecompressive 465 488 622 394 394 486 properties stress (MPa) afterchemical Depth of surface 83 42 30 37 22 15 tempering compressive stresslayer (μm) Transmittance: 91 91 91 90.8 90.8 90.8 428 nm (%)Transmittance ratio: 0.998 0.998 0.998 0.993 0.993 0.993 428 nm/650 nmFluorescent X-ray 0 0 0 0 0 0 Ag intensity (μm/cm²) AntibacterialAntibacterial Polished Polished Polished Polished Polished Polishedtreatment surface surface surface surface surface surface surfaceconditions Firing 350 350 350 350 350 350 temperature (° C.) Firing time(h) 15 15 15 15 15 15 Glass Surface compressive 455 462 570 404 424 489substrate stress (MPa) properties Depth of surface 84 44 31 36 23 14(after chemical compressive tempering and stress layer (μm)antibacterial Transmittance: 88.4 90.7 90.8 90.3 90.3 90.9 treatment)428 nm (%) Transmittance ratio: 0.993 1.00 1.00 0.992 0.993 0.994 428nm/650 nm Fluorescent X-ray 2.2 1.7 2.7 0.45 0.40 0.45 Ag intensity(μg/cm²)

TABLE 5 Ex. 19 Ex. 20 Ex. 21 Glass Type of glass Glass A Glass A Glass Asubstrate Thickness (mm) 0.32 0.32 0.32 Substrate Surface compressivestress 0 0 0 properties (MPa) before Depth of surface compressive 0 0 0chemical stress layer (μm) tempering Transmittance: 428 nm (%) 91 91 91Transmittance ratio: 0.996 0.996 0.996 428 nm/650 nm Fluorescent X-rayAg 0 0 0 intensity (μm/cm²) Chemical KNO₃ (mass %) 99.9 99.9 99.9tempering NaNO₃ (mass %) 0 0 0 treatment AgNO₃ (mass %) 0.1 0.1 0.1 andTreatment temperature 460 460 460 antibacterial (° C.) treatmentTreatment time (h) 1 16 24 conditions Glass Surface compressive stress323 221 211 substrate (MPa) properties Depth of surface compressive 33 —— (after stress layer (μm) chemical Transmittance: 428 nm (%) 85.2 66.259.2 tempering Transmittance ratio: 0.941 0.747 0.677 and 428 nm/650 nmantibacterial Fluorescent X-ray Ag 147.7 185.3 185.9 treatment)intensity (μg/cm²)

Each of the glass substrates (Examples of the present invention) of thepresent invention obtained had a ratio (T1/T2) of the transmittance T1at a wavelength of 428 nm to the transmittance T2 at a wavelength of 650nm of the glass substrate of at least 0.95, and a transmittance at awavelength of 428 nm of at least 86%, and had a high transparency and ahigh visible transmittance suitable as a glass substrate for a displaycover glass. Further, it had a depth of the surface compressive stresslayer of at least 3 μm, a surface compressive stress of at least 250 MPaand a silver amount at a depth of 40 μm from the glass substrate surfaceof from 0.2 to 100 μg/cm², and is considered to have a high strength andantibacterial properties. Whereas the glass substrate in Example 6(Comparative Example) had no surface compressive stress layer on theglass substrate surface and had insufficient strength, since chemicaltempering treatment was not conducted. The glass substrate in Example 7(Comparative Example) had a low surface compressive stress andinsufficient strength, and had a low transmittance at a wavelength of428 nm and a low transmittance ratio (T1/T2), and was insufficient as aglass substrate for a display cover glass in view of the transparencyand the visible transmittance. It is considered to be because in theglass substrate in which no sufficient surface compressive stress isformed by the chemical tempering treatment, diffusion of silver ions isaccelerated by the antibacterial treatment as potassium ions have alarger ionic radius than silver ions, and coloring of the glasssubstrate occurred by silver colloid resultingly.

Further, each of the glass substrates in Examples 19 to 21 (ComparativeExamples) had a low transmittance at a wavelength of 428 nm and a lowtransmittance ratio (T1/T2), and was insufficient as a glass substratefor a display cover glass in view of the transparency and the visibletransmittance. This is considered to be because silver ions wereexcessively diffused in the glass substrate surface by conducting thechemical tempering treatment and the antibacterial treatmentsimultaneously, whereby coloring of glass by occurrence of silvercolloid was remarkable, and optical properties of glass weredeteriorated.

Then, with respect to the non-polished glass A plate-formed by the floatprocess, the difference in the glass substrate properties between caseswhere an antibacterial substance-containing layer was provided on thetin-side surface and on the opposite side to the tin-side surface, wasconfirmed.

First, chemical tempering treatment was applied to glass A having athickness of 0.55 mm to prepare a glass substrate having a surfacecompressive stress of 441 MPa, a thickness of the surface compressivestress layer of 7 μm, a transmittance (wavelength: 428 nm) of 91%, atransmittance ratio (T1/T2) of 0.996 and a fluorescent X-ray Agintensity of 0 μg/cm². With respect to such a glass substrate,antibacterial treatment was conducted on the tin-side surface and on theopposite side to the tin-side surface under the respective conditions,and the properties of the obtained glass substrate was examined. Theantibacterial treatment conditions and the glass substrate properties inExamples and Comparative Examples thus obtained are shown in Tables 6and 7. In Tables, Examples 22 to 29 and 30 to 35 are Examples of thepresent invention, and Examples 36 and 37 are Comparative Examples.

TABLE 6 Ex. 22 Ex. 23 Ex. 24 Ex. 25 Ex. 26 Ex. 27 Ex. 28 Ex. 29 Ex. 30Glass Type of glass Glass A Glass A Glass A Glass A Glass A Glass AGlass A Glass A Glass A substrate Thickness (mm) 0.55 0.55 0.55 0.550.55 0.55 0.55 0.55 0.55 Antibacterial Antibacterial-treated Oppositeside to tin-side surface treatment surface conditions Firing 250 300 350350 350 350 400 450 500 temperature (° C.) Firing time (h) 15 15 5 15 3060 15 15 15 Glass Surface compressive 433 409 441 429 438 441 401 295 67substrate stress (MPa) properties Depth of surface 8 8 9.3 9.3 7.5 7.59.4 9.8 19.6 (after chemical compressive tempering and stress layer (μm)antibacterial Transmittance: 90.2 90.0 89.9 89.7 90.1 90.1 89.7 90.287.6 treatment) 428 nm (%) Transmittance ratio: 0.997 0.996 0.996 0.9950.998 0.998 0.998 0.996 0.968 428 nm/650 nm Fluorescent X-ray 0.5 1.21.8 1.8 2.0 2.4 3.7 10.8 20.3 Ag intensity (μg/cm²)

TABLE 7 Ex. 31 Ex. 32 Ex. 33 Ex. 34 Ex. 35 Ex. 36 Ex. 37 Glass Type ofglass Glass A Glass A Glass A Glass A Glass A Glass A Glass A substrateThickness (mm) 0.55 0.55 0.55 0.55 0.55 0.55 0.55 AntibacterialAntibacterial- Tin-side surface treatment treated surface conditionsFiring 350 350 350 350 400 450 500 temperature (° C.) Firing time (h) 515 30 60 15 15 15 Glass Surface compressive 438 435 446 427 407 296 32substrate stress (MPa) properties Depth of surface 5.9 7.6 5.8 6 5.9 8.99.7 (after chemical compressive tempering and stress layer (μm)antibacterial Transmittance: 89.5 89.8 89.3 88.8 86.0 70.8 52.0treatment) 428 nm (%) Transmittance ratio: 0.992 0.994 0.993 0.985 0.9560.802 0.604 428 nm/650 nm Fluorescent X-ray 2.0 1.9 2.1 2.7 4.4 12.923.6 Ag intensity (μg/cm²)

From the obtained results, in a case where the antibacterial treatmentwas conducted on the tin-side surface, in Examples 36 and 37 (bothComparative Examples) in which the firing temperature was high (at least450° C.), glass was colored and the transmittance at a wavelength of 428nm and the transmittance ratio (T1/T2) were very low. This is consideredto be because the tin component diffused in the glass substrate surfaceon the tin-side surface reduced silver in the silver ion diffusion layerwhich was the antibacterial substance-containing layer to form silvercolloid, which colored glass. Whereas in Examples 31 to 35 (Examples ofthe present invention) in which the antibacterial treatment wasconducted on the tin-side surface, it is considered that thetransmittance was not low as the firing temperature was low and theoccurrence of silver colloid was thereby suppressed.

Further, in Examples 30 and 37 in which the firing temperature in theantibacterial treatment was high, the surface compressive stress wasvery low. This is considered to be because the surface compressivestress generated in the chemical tempering treatment was relaxed byfiring. Whereas in Examples of the present invention (Examples 22 to 29and 31 to 35) in which the antibacterial treatment was conducted at afiring temperature of at most 475° C., no remarkable decrease of thesurface compressive stress was observed, and the obtained glasssubstrate had a high strength.

INDUSTRIAL APPLICABILITY

According to the present invention, it is possible to provide a glasssubstrate for a display cover glass not only having excellent strengthand antibacterial properties but also having a high transparency and ahigh visible transmittance by suppressing coloring of glass due tosilver colloid.

This application is a continuation of PCT Application No.PCT/JP2010/070621, filed on Nov. 18, 2010, which is based upon andclaims the benefit of priority from Japanese Patent Application No.2009-267869 filed on Nov. 25, 2009. The contents of those applicationsare incorporated herein by reference in its entirety.

1. A glass substrate for a display cover glass, which comprises asurface compressive stress layer and an antibacterialsubstance-containing layer on the glass substrate surface, characterizedby having a ratio (T1/T2) of the transmittance T1 at a wavelength of 428nm to the transmittance T2 at a wavelength of 650 nm of the glasssubstrate of at least 0.95, and a transmittance at a wavelength of 428nm of at least 86% when the thickness of the glass substrate is from 0.1to 3.0 mm.
 2. The glass substrate for a display cover glass according toclaim 1, wherein the glass substrate has a glass composition comprising,as represented by mol % as calculated as oxides, from 55 to 80% of SiO₂,from 0.1 to 15% of Al₂O₃, from 0 to 15% of B₂O₃, from 0 to 10% of ZnO,from 0.1 to 15% of Na₂O, from 0 to 10% of K₂O, and from 0 to 16% ofMgO+CaO.
 3. The glass substrate for a display cover glass according toclaim 1, wherein the surface compressive stress layer on the glasssubstrate surface is formed by chemical tempering, and the surfacecompressive stress layer has a depth of at least 3 μm and a surfacecompressive stress of a least 250 MPa.
 4. The glass substrate for adisplay cover glass according to claim 1, wherein the antibacterialsubstance-containing layer is a silver ion diffusion layer having silverions diffused in the glass substrate surface.
 5. The glass substrate fora display cover glass according to claim 4, wherein the silver iondiffusion layer has a silver amount of from 0.2 to 100 μg/cm² at a depthof 40 μm from the glass substrate surface.
 6. The glass substrate for adisplay cover glass according to claim 1, wherein the glass substrate isplate-formed by a float process.
 7. The glass substrate for a displaycover glass according to claim 1, which is used for a cover glass of atouch panel display.
 8. A display device, which uses the glass substratefor a display cover glass as defined in claim 1 as a front glass of adisplay. 9.-12. (canceled)